Evidence map›Paper›PMID 21177646›Full record

ArticleNucleic acids research2011

Arxes: retrotransposed genes required for adipogenesis.

Andreas Prokesch, Juliane G Bogner-Strauss, Hubert Hackl, Dietmar Rieder, Claudia Neuhold, Evelyn Walenta, Anne Krogsdam, Marcel Scheideler, Christine Papak, Wing-Cheong Wong and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  7. Critical role of the peroxisomal protein PEX16 in white adipocyte development and lipid homeostasis.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2017
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 2 countries.

Andreas ProkeschInstitute for Genomics and Bioinformatics, Graz University of Technology, Biocenter, Austria. andreas.prokesch@tugraz.at
Juliane G Bogner-Strauss
Hubert Hackl
Dietmar Rieder
Claudia Neuhold
Evelyn Walenta
Anne Krogsdam
Marcel Scheideler
Christine Papak
Wing-Cheong Wong
Charles Vinson
Frank Eisenhaber
Zlatko Trajanoski
Agency for Science, Technology and Research · SGVienna Biocenter · AT

Funding

Austrian Science Fund FWF W 1226
6 · The paper itself

Abstract

Retrotransposed sequences arise from messenger RNAs (mRNAs) that have been reinserted into genomic DNA by reverse transcription. Usually, these sequences are embedded in dormant regions, collect missense mutations over time and constitute processed, nonfunctional pseudogenes. There are thousands of processed pseudogenes in the mouse and human genome. Here, we report evidence for two paralog genes (termed Arxes1 and Arxes2), which arose by retrotransposition of the signal peptidase Spcs3 followed by a segmental duplication event. They gained a functional promoter that we show to be transactivated by adipogenic transcription factors. We further show that the Arxes mRNAs are highly expressed in adipose tissue and strongly upregulated during adipogenesis in different cell models. Additionally, their expression is elevated by an anti-diabetic agent in vitro and in vivo. Importantly, we provide evidence that the Arxes genes are translated and that the proteins are located in the endoplasmic reticulum. Although the sequence similarity and subcellular location are reminiscent of their parental gene, our data suggest that the Arxes have developed a different function, since their expression is required for adipogenesis, whereas Spcs3 is dispensable. In summary, we report retrotransposed-duplicated genes that evolved from a parental gene to function in a tissue and adipogenesis-specific context.

Indexed as

Retroelements3T3-L1 CellsAdipogenesisAdipose TissueAnimalsCCAAT-Enhancer-Binding ProteinsCells, CulturedGene Expression ProfilingGenomicsHypoglycemic AgentsMaleMiceMice, Inbred C57BLOsteoblastsOsteogenesisPeptide HydrolasesArxes1 protein, mouseArxes2 protein, mouseCCAAT-Enhancer-Binding ProteinsHypoglycemic AgentsPeptide HydrolasesPPAR gammaRetroelementsRNA, Messenger

Identifiers

PMID21177646
PMCPMC3082915
OpenAlexW2107023092

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.